Ust the protein chain in the electron density. After several rounds of model rebuilding and intermittent Pentagastrin site cycles of refinement, Rcryst factor dropped to 0.282. The group temperature factor (B) refinement was used with further model adjustments yielding Rcryst factor of 26.3 . The difference Fourier (Fo2Fc) map computed at this stage revealed additional non-protein but quite characteristic electron densities at 2s cutoffs at two sites which were located atWide Spectrum Antimicrobial Role of Camel PGRP-SFigure 4. Structure of the ternary complex of CPGRP-S with LPS and LTA. The binding sites are shown in different colours. SA and LPS are shown as space fitting models in blue and green colours respectively. doi:10.1371/journal.pone.0053756.gInhibition of LPS and SA Induced Expressions of TNFa and IFN-cThe recognition of LPS by immune cells is a significant component of the acute adaptive and memory immune response. The critical indicators of the pathogenesis of bacterial infection are the copious amount of production of pro-inflammatory buy Tubastatin A cytokines TNF-a and IFN-c predominantly by macrophages and T cells. In order to determine the efficiency of CPGRP-S to inhibit the production of pro-inflammatory cytokines such as TNF-a and IFN-c, the cultured PBMCs were challenged with the mixture of LPS and SA and the observed pro-inflammatory cytokines were assayed in the cultured PBMCs. The treatment of PBMCs with 10 mg/ml of LPS and SA mixture increased the production of TNF-a and IFN-c by 6.2 and 7.5 folds respectively (Figure 3) in comparison to media alone. The increased levels of TNF-a and IFN-c were almost completely abolished when the 
cells were incubated with 10 mg/ml of LPS and SA mixture along with 5 mg/ml of CPGRP-S. This indicated that CPGRP-S inhibited the pro-inflammatory effects of LPS and SA.Overall StructureCrystal structure of CPGRP-S consists of four crystallographically independent molecules A, B, C and D in the asymmetric unit in associations as A and C dimers (Figure 4). An examination of the intermolecular interactions of the packing of molecules in the crystal together with the buried surface areas between them indicated that A 125-65-5 interface provided the most stable association ?with an approximate buried surface area of 798 A2 while C interface was slightly less 
stable with a buried surface area of ?702 A2. The A and B interfaces were found to be weakly??associated with buried surface areas of 340 A2 and 111 A2 respectively. A further examination of the packing of molecules in the crystal revealed that the interface between Oltipraz custom synthesis molecule D and 
its symmetry related molecule D9 and also molecule C and its symmetry 24786787 related molecule C9 showed identical buried areas as that of A interface. In fact, it represented the same contact as represented by A and B monomers. It showed that one surface of monomer formed A interface while its opposite surface was part of the C interface. Both these surfaces of the monomer are located on opposite sides of the monomer. Thus the structure of CPGRP-S can be described as a contiguous chain of protein molecules in which A and C contacts occur alternatingly (Figure 5). The molecular mass of the first peak in the elution profile obtained using size exclusion chromatography was estimated based on the void volume. This value was similar to that determined by extrapolating the value of hydrodynamic radii observed using dynamic light scattering of the protein [19]. These values were similar to that derived.Ust the protein chain in the electron density. After several rounds of model rebuilding and intermittent cycles of refinement, Rcryst factor dropped to 0.282. The group temperature factor (B) refinement was used with further model adjustments yielding Rcryst factor of 26.3 . The difference Fourier (Fo2Fc) map computed at this stage revealed additional non-protein but quite characteristic electron densities at 2s cutoffs at two sites which were located atWide Spectrum Antimicrobial Role of Camel PGRP-SFigure 4. Structure of the ternary complex of CPGRP-S with LPS and LTA. The binding sites are shown in different colours. SA and LPS are shown as space fitting models in blue and green colours respectively. doi:10.1371/journal.pone.0053756.gInhibition of LPS and SA Induced Expressions of TNFa and IFN-cThe recognition of LPS by immune cells is a significant component of the acute adaptive and memory immune response. The critical indicators of the pathogenesis of bacterial infection are the copious amount of production of pro-inflammatory cytokines TNF-a and IFN-c predominantly by macrophages and T cells. In order to determine the efficiency of CPGRP-S to inhibit the production of pro-inflammatory cytokines such as TNF-a and IFN-c, the cultured PBMCs were challenged with the mixture of LPS and SA and the observed pro-inflammatory cytokines were assayed in the cultured PBMCs. The treatment of PBMCs with 10 mg/ml of LPS and SA mixture increased the production of TNF-a and IFN-c by 6.2 and 7.5 folds respectively (Figure 3) in comparison to media alone. The increased levels of TNF-a and IFN-c were almost completely abolished when the cells were incubated with 10 mg/ml of LPS and SA mixture along with 5 mg/ml of CPGRP-S. This indicated that CPGRP-S inhibited the pro-inflammatory effects of LPS and SA.Overall StructureCrystal structure of CPGRP-S consists of four crystallographically independent molecules A, B, C and D in the asymmetric unit in associations as A and C dimers (Figure 4). An examination of the intermolecular interactions of the packing of molecules in the crystal together with the buried surface areas between them indicated that A interface provided the most stable association ?with an approximate buried surface area of 798 A2 while C interface was slightly less stable with a buried surface area of ?702 A2. The A and B interfaces were found to be weakly??associated with buried surface areas of 340 A2 and 111 A2 respectively. A further examination of the packing of molecules in the crystal revealed that the interface between molecule D and its symmetry related molecule D9 and also molecule C and its symmetry 24786787 related molecule C9 showed identical buried areas as that of A interface. In fact, it represented the same contact as represented by A and B monomers. It showed that one surface of monomer formed A interface while its opposite surface was part of the C interface. Both these surfaces of the monomer are located on opposite sides of the monomer. Thus the structure of CPGRP-S can be described as a contiguous chain of protein molecules in which A and C contacts occur alternatingly (Figure 5). The molecular mass of the first peak in the elution profile obtained using size exclusion chromatography was estimated based on the void volume. This value was similar to that determined by extrapolating the value of hydrodynamic radii observed using dynamic light scattering of the protein [19]. These values were similar to that derived.Ust the protein chain in the electron density. After several rounds of model rebuilding and intermittent cycles of refinement, Rcryst factor dropped to 0.282. The group temperature factor (B) refinement was used with further model adjustments yielding Rcryst factor of 26.3 . The difference Fourier (Fo2Fc) map computed at this stage revealed additional non-protein but quite characteristic electron densities at 2s cutoffs at two sites which were located atWide Spectrum Antimicrobial Role of Camel PGRP-SFigure 4. Structure of the ternary complex of CPGRP-S with LPS and LTA. The binding sites are shown in different colours. SA and LPS are shown as space fitting models in blue and green colours respectively. doi:10.1371/journal.pone.0053756.gInhibition of LPS and SA Induced Expressions of TNFa and IFN-cThe recognition of LPS by immune cells is a significant component of the acute adaptive and memory immune response. The critical indicators of the pathogenesis of bacterial infection are the copious amount of production of pro-inflammatory cytokines TNF-a and IFN-c predominantly by macrophages and T cells. In order to determine the efficiency of CPGRP-S to inhibit the production of pro-inflammatory cytokines such as TNF-a and IFN-c, the cultured PBMCs were challenged with the mixture of LPS and SA and the observed pro-inflammatory cytokines were assayed in the cultured PBMCs. The treatment of PBMCs with 10 mg/ml of LPS and SA mixture increased the production of TNF-a and IFN-c by 6.2 and 7.5 folds respectively (Figure 3) in comparison to media alone. The increased levels of 
TNF-a and IFN-c were almost completely abolished when the cells were incubated with 10 mg/ml of LPS and SA mixture along with 5 mg/ml of CPGRP-S. This indicated that CPGRP-S inhibited the pro-inflammatory effects of LPS and SA.Overall StructureCrystal structure of CPGRP-S consists of four crystallographically independent molecules A, B, C and D in the asymmetric unit in associations as A and C dimers (Figure 4). An examination of the intermolecular interactions of the packing of molecules in the crystal together with the buried surface areas between them indicated that A interface provided the most stable association ?with an approximate buried surface area of 798 A2 while C interface was slightly less stable with a buried surface area of ?702 A2. The A and B interfaces were found to be weakly??associated with buried surface areas of 340 A2 and 111 A2 respectively. A further examination of the packing of molecules in the crystal revealed that the interface between molecule D and its symmetry related molecule D9 and also molecule C and its symmetry 24786787 related molecule C9 showed identical buried areas as that of A interface. In fact, it represented the same contact as represented by A and B monomers. It showed that one surface of monomer formed A interface while its opposite surface was part of the C interface. Both these surfaces of the monomer are located on opposite sides of the monomer. Thus the structure of CPGRP-S can be described as a contiguous chain of protein molecules in which A and C contacts occur alternatingly (Figure 5). The molecular mass of the first peak in the elution profile obtained using size exclusion chromatography was estimated based on the void volume. This value was similar to that determined by extrapolating the value of hydrodynamic radii observed using dynamic light scattering of the protein [19]. These values were similar to that derived.Ust the protein chain in the electron density. After several rounds of model rebuilding and intermittent cycles of refinement, Rcryst factor dropped to 0.282. The group temperature factor (B) refinement was used with further model adjustments yielding Rcryst factor of 26.3 . The difference Fourier (Fo2Fc) map computed at this stage revealed additional non-protein but quite characteristic electron densities at 2s cutoffs at two sites which were located atWide Spectrum Antimicrobial Role of Camel PGRP-SFigure 4. Structure of the ternary complex of CPGRP-S with LPS and LTA. The binding sites are shown in different colours. SA and LPS are shown as space fitting models in blue and green colours respectively. doi:10.1371/journal.pone.0053756.gInhibition of LPS and SA Induced Expressions of TNFa and IFN-cThe recognition of LPS by immune cells is a significant component of the acute adaptive and memory immune response. The critical indicators of the pathogenesis of bacterial infection are the copious amount of production of pro-inflammatory cytokines TNF-a and IFN-c predominantly by macrophages and T cells. In order to determine the efficiency of CPGRP-S to inhibit the production of pro-inflammatory cytokines such as TNF-a and IFN-c, the cultured PBMCs were challenged with the mixture of LPS and SA and the observed pro-inflammatory cytokines were assayed in the cultured PBMCs. The treatment of PBMCs with 10 mg/ml of LPS and SA mixture increased the production of TNF-a and IFN-c by 6.2 and 7.5 folds respectively (Figure 3) in comparison to media alone. The increased levels of TNF-a and IFN-c were almost completely abolished when the cells were incubated with 10 mg/ml of LPS and SA mixture along with 5 mg/ml of CPGRP-S. This indicated that CPGRP-S inhibited the pro-inflammatory effects of LPS and SA.Overall StructureCrystal structure of CPGRP-S consists of four crystallographically independent molecules A, B, C and D in the asymmetric unit in associations as A and C dimers (Figure 4). An examination of the intermolecular interactions of the packing of molecules in the crystal together with the buried surface areas between them indicated that A interface provided the most stable association ?with an approximate buried surface area of 798 A2 while C interface was slightly less stable with a buried surface area of ?702 A2. The A and B interfaces were found to be weakly??associated with buried surface areas of 340 A2 and 111 A2 respectively. A further examination of the packing of molecules in the crystal revealed that the interface between molecule D and its symmetry related molecule D9 and also molecule C and its symmetry 24786787 related molecule C9 showed identical buried areas as that of A interface. In fact, it represented the same contact as represented by A and B monomers. It showed that one surface of monomer formed A interface while its opposite surface was part of the C interface. Both these surfaces of the monomer are located on opposite sides of the monomer. Thus the structure of CPGRP-S can be described as a contiguous chain of protein molecules in which A and C contacts occur alternatingly (Figure 5). The molecular mass of the first peak in the elution profile obtained using size exclusion chromatography was estimated based on the void volume. This value was similar to that determined by extrapolating the value of hydrodynamic radii observed using dynamic light scattering of the protein [19]. These values were similar to that derived.
